Pituitary tumor transforming gene (PTTG) is a newly identified transforming
gene, the functional mechanism of which is little understood. Computationa
l analysis reveals a C terminus rich in Glu and Pro, a known characteristic
of transcriptional activation domains. We report here that murine PTTG ind
eed possesses transactivation ability, which correlates highly with its tra
nsforming properties. Pro(139), Ser(159) pro(157) pro(158) -Ser(159)-Pro(16
0) (PPXP motif), and Leu(120)-Asp(121)-phe(122)- Asp(123)-Leu(124) Were fou
nd to be important for transarctivation. Mutation to Ala at a key Pro(139)
residue not only disrupted the transactivation function but also resulted i
n the loss of transforming ability in NIH3T3 cells. A murine PTTG cDNA that
encodes a variant C-terminal tail (Gly-Lys-Gly-Val-Arg-Ser-Asn-Gly-Cys-Lys
-Asp-Leu- Val-Thr) was cloned. This novel PTTG is devoid of transactivation
and transforming ability; deletion of its variant C-terminal tail restores
both transactivation and transforming ability. These results show a high c
orrelation between the transforming and transactivation functions of PTTG a
nd also indicate that the novel PTTG variant may function as an endogenous
competitor to wild-type PTTG.